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Inhibitors of Viral Protein Synthesis

Protein synthesis is indispensable for viral replication, as viruses lack the cellular machinery required for this process and must hijack the host's translational apparatus. In response, host cells deploy a critical innate immune defense involving interferons, specialized cytokines that play a central role in inhibiting viral propagation.Upon viral detection, infected cells release interferons that bind to receptors on adjacent uninfected cells, activating the JAK-STAT signaling pathway and...
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Related Experiment Video

Updated: Jun 16, 2026

Zika Virus Infectious Cell Culture System and the In Vitro Prophylactic Effect of Interferons
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Published on: August 23, 2016

Ribavirin plus interferon versus interferon for chronic hepatitis C.

Jesper Brok1, Lise Lotte Gluud, Christian Gluud

  • 1Cochrane Hepato-Biliary Group, Copenhagen Trial Unit, Centre for Clinical Intervention Research, Department 3344, Rigshospitalet, Copenhagen University Hospital, Blegdamsvej 9, Copenhagen, Denmark, DK-2100.

The Cochrane Database of Systematic Reviews
|January 22, 2010
PubMed
Summary

Combination therapy with ribavirin and interferon is more effective for clearing hepatitis C virus (HCV) than interferon alone. However, it increases adverse reactions, and more evidence is needed to confirm benefits for liver morbidity and mortality.

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Area of Science:

  • Hepatology
  • Virology
  • Clinical Pharmacology

Background:

  • Hepatitis C virus (HCV) infection is a leading cause of liver disease and death.
  • Standard treatment involves pegylated interferon and ribavirin, but its clinical impact remains debated.

Purpose of the Study:

  • To evaluate the efficacy and safety of combining ribavirin with interferon versus interferon monotherapy for chronic hepatitis C.
  • To assess effects on viral clearance, liver-related morbidity, mortality, and adverse events.

Main Methods:

  • Systematic review and meta-analysis of 83 randomized controlled trials involving 12,707 patients.
  • Inclusion of trials regardless of blinding, language, or publication status.
  • Primary outcomes included sustained virological response, liver morbidity, mortality, and adverse events; subgroup analyses were performed.

Main Results:

  • Combination therapy significantly improved sustained virological response across all patient subgroups (naive, relapsers, non-responders).
  • Combined treatment reduced liver morbidity and all-cause mortality in the overall patient group, though not significantly in subgroups.
  • Increased risks of hematological, dermatological, gastrointestinal, infectious, and miscellaneous adverse events were observed, leading to higher discontinuation and dose reduction rates.

Conclusions:

  • Ribavirin plus interferon demonstrates superior efficacy in achieving viral clearance compared to interferon monotherapy.
  • While combination therapy may reduce liver-related morbidity and mortality, further evidence is required.
  • The benefit-risk ratio must be carefully considered due to significant adverse reactions, increased treatment discontinuations, and associated costs.